Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51078 |
| ensemblid | ENSG00000176946.13 |
| hgncid | 23187 |
| symbol | THAP4 |
| name | THAP domain containing 4 |
| refseq_nuc | NM_015963.6 |
| refseq_prot | NP_057047.4 |
| ensembl_nuc | ENST00000407315.6 |
| ensembl_prot | ENSP00000385006.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 241584405 |
| end | 241637158 |
| strand | - |
| ver | v1.2 |
| region | chr2:241584405-241637158 |
| region5000 | chr2:241579405-241642158 |
| regionname0 | THAP4_chr2_241584405_241637158 |
| regionname5000 | THAP4_chr2_241579405_241642158 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 577 | 274 | 52 | 36 | 157 | 5 | 23 | 124 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| a0002 | 1/0 | 577 | 112 | 41 | 26 | 20 | 9 | 15 | 14 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| a0003 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| a0004 | 0/0 | 577 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| a0005 | 0/0 | 577 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| a0006 | 0/0 | 577 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | MVICC others(572): Show |
chr2 | 241579405 | 241642158 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1731 | 139 | 36 | 25 | 68 | 3 | 6 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0001c0002 | 0/0 | 1731 | 134 | 16 | 11 | 89 | 2 | 16 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0001c0009 | 0/0 | 1731 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0002c0003 | 1/0 | 1731 | 75 | 23 | 17 | 14 | 9 | 11 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0002c0004 | 0/0 | 1731 | 33 | 14 | 9 | 6 | 0 | 4 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0002c0005 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0002c0006 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0003c0008 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0004c0011 | 0/0 | 1731 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0005c0010 | 0/0 | 1731 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 | ||
| a0006c0007 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATGGT others(1726): Show |
chr2 | 241579405 | 241642158 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2076 | 134 | 36 | 23 | 65 | 3 | 6 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0001c0001t0002 | 0/0 | 2076 | 5 | 0 | 2 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0001c0002t0001 | 0/0 | 2076 | 131 | 16 | 11 | 86 | 2 | 16 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0001c0002t0004 | 0/0 | 2084 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2079): Show |
chr2 | 241579405 | 241642158 |
| a0001c0009t0001 | 0/0 | 2076 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0003t0001 | 1/0 | 2076 | 74 | 22 | 17 | 14 | 9 | 11 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0003t0002 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0004t0001 | 0/0 | 2076 | 27 | 13 | 5 | 6 | 0 | 3 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0004t0003 | 0/0 | 2076 | 5 | 0 | 4 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0004t0005 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0005t0001 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0002c0006t0001 | 0/0 | 2076 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0003c0008t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0004c0011t0001 | 0/0 | 2076 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0005c0010t0001 | 0/0 | 2076 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| a0006c0007t0001 | 0/0 | 2076 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | ATCTT others(2071): Show |
chr2 | 241579405 | 241642158 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0002t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0001c0009t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0003t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0004t0005g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0002c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0003c0008t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0004c0011t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0005c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| a0006c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0087 | EUR | GBR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0299 | EUR | GBR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0196 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0091 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00544 | hp1 | a0002 | c0004 | t0001 | g0167 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00544 | hp2 | a0002 | c0003 | t0001 | g0194 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0083 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0240 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0101 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0098 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0090 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0017 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01081 | hp1 | a0002 | c0004 | t0003 | g0159 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01099 | hp2 | a0002 | c0003 | t0001 | g0263 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01106 | hp2 | a0003 | c0008 | t0001 | g0073 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01167 | hp1 | a0002 | c0004 | t0001 | g0077 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0193 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01169 | hp1 | a0002 | c0004 | t0001 | g0074 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0183 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0286 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0185 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0182 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0165 | AMR | PUR | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0086 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0181 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01261 | hp1 | a0002 | c0003 | t0001 | g0092 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01261 | hp2 | a0002 | c0004 | t0003 | g0164 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01346 | hp1 | a0004 | c0011 | t0001 | g0239 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0017 | EUR | IBS | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0261 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01891 | hp1 | a0002 | c0004 | t0001 | g0278 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01891 | hp2 | a0002 | c0006 | t0001 | g0157 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0176 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0324 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0175 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0187 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02004 | hp2 | a0002 | c0004 | t0003 | g0163 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0337 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0100 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0258 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0346 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02129 | hp1 | a0005 | c0010 | t0001 | g0034 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02258 | hp1 | a0006 | c0007 | t0001 | g0072 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0276 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0280 | AMR | PEL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02451 | hp1 | a0002 | c0004 | t0001 | g0162 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0080 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | KHV | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02572 | hp1 | a0002 | c0004 | t0001 | g0171 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0093 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02602 | hp1 | a0001 | c0009 | t0001 | g0335 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0099 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0266 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0076 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0088 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0265 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02683 | hp1 | a0002 | c0003 | t0001 | g0184 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0094 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02738 | hp1 | a0002 | c0004 | t0001 | g0172 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0342 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02818 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02886 | hp2 | a0002 | c0004 | t0001 | g0009 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0180 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0173 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0067 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0178 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0302 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03130 | hp2 | a0002 | c0004 | t0001 | g0071 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03139 | hp1 | a0002 | c0006 | t0001 | g0156 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03209 | hp1 | a0002 | c0004 | t0005 | g0350 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0166 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0155 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03490 | hp1 | a0002 | c0004 | t0003 | g0161 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0317 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0289 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0318 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0170 | AFR | ESN | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0279 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03540 | hp2 | a0002 | c0004 | t0001 | g0158 | AFR | GWD | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03579 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03579 | hp2 | a0002 | c0004 | t0001 | g0060 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0177 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0023 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0314 | SAS | PJL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0300 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0085 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0328 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0096 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04115 | hp1 | a0002 | c0004 | t0001 | g0277 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0321 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0319 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0361 | SAS | BEB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0244 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0084 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | STU | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0356 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0355 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18964 | hp1 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18974 | hp1 | a0001 | c0002 | t0004 | g0364 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18981 | hp1 | a0001 | c0002 | t0004 | g0362 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0168 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18999 | hp1 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19000 | hp2 | a0002 | c0004 | t0001 | g0169 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19009 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0020 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0205 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19055 | hp1 | a0001 | c0002 | t0004 | g0363 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19055 | hp2 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0325 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0354 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | ASW | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ASW | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0264 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0186 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0082 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0202 | EUR | TSI | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0103 | SAS | GIH | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | GIH | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01123 | hp1 | a0002 | c0004 | t0003 | g0160 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0095 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0262 | AFR | ACB | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG03471 | hp2 | a0002 | c0005 | t0001 | g0154 | AFR | MSL | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | USA | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0359 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0081 | AFR | LWK | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0236 | REF | REF | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0179 | REF | REF | THAP4_chr2_241579405_241642158 | THAP4 | chr2 | 241579405 | 241642158 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241601937 | T | C | 1 | a0005 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.1573A>G | p.Ile525Val | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/6 | 1714/2076 | 1573/1734 | 525/577 | chr2 | 241601937 | |||
| chr2:241633535 | C | G | 1 | a0003 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.622G>C | p.Gly208Arg | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 763/2076 | 622/1734 | 208/577 | chr2 | 241633535 | |||
| chr2:241633596 | C | A | 1 | a0004 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.561G>T | p.Gln187His | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 702/2076 | 561/1734 | 187/577 | chr2 | 241633596 | |||
| chr2:241633796 | T | C | 3 | a0001 a0004 a0005 |
275 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(272): Show |
missense_variant | MODERATE | c.361A>G | p.Ser121Gly | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 502/2076 | 361/1734 | 121/577 | chr2 | 241633796 | |||
| chr2:241633807 | C | T | 1 | a0006 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.350G>A | p.Ser117Asn | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 491/2076 | 350/1734 | 117/577 | chr2 | 241633807 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241603055 | C | T | 1 | a0001c0009 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1425G>A | p.Thr475Thr | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/6 | 1566/2076 | 1425/1734 | 475/577 | chr2 | 241603055 | |||
| chr2:241633278 | C | T | 1 | a0002c0006 | 2 | HG01891.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.879G>A | p.Pro293Pro | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 1020/2076 | 879/1734 | 293/577 | chr2 | 241633278 | |||
| chr2:241633284 | C | T | 1 | a0002c0005 | 2 | HG03453.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.873G>A | p.Ala291Ala | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 1014/2076 | 873/1734 | 291/577 | chr2 | 241633284 | |||
| chr2:241633431 | A | G | 5 | a0001c0002 a0001c0009 a0002c0004 others(2): Show |
172 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(169): Show |
synonymous_variant | LOW | c.726T>C | p.Ser242Ser | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/6 | 867/2076 | 726/1734 | 242/577 | chr2 | 241633431 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241584508 | C | G | 1 | a0002c0004t0003 | 5 | HG01081.hp1 HG01123.hp1 HG01261.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*98G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 98 | chr2 | 241584508 | ||||||
| chr2:241584527 | C | T | 1 | a0002c0004t0005 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 79 | chr2 | 241584527 | ||||||
| chr2:241584528 | G | A | 2 | a0001c0001t0002 a0002c0003t0002 |
6 | HG01884.hp1 HG01981.hp1 HG02293.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*78C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 6/6 | 78 | chr2 | 241584528 | ||||||
| chr2:241637059 | G | GCCGCCCG others(1): Show |
1 | a0001c0002t0004 | 3 | NA18974.hp1 NA18981.hp1 NA19055.hp1 |
5_prime_UTR_variant | MODIFIER | c.-50_-43dupGCGGGCGG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/6 | 43 | chr2 | 241637059 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:241584991 | C | T | 4 | a0001c0002t0001g0025 a0001c0002t0004g0362 a0001c0002t0004g0363 others(1): Show |
4 | NA18974.hp1 NA18981.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-266G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241584991 | |||||||
| chr2:241585172 | G | A | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1615-447C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585172 | |||||||
| chr2:241585241 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1615-516C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585241 | |||||||
| chr2:241585279 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0002c0003t0001g0181 |
3 | HG01258.hp1 HG02080.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1615-554G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585279 | |||||||
| chr2:241585498 | A | G | 5 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0002c0004t0001g0074 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-773T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585498 | |||||||
| chr2:241585546 | G | A | 3 | a0001c0001t0001g0216 a0002c0003t0001g0173 a0002c0003t0001g0174 |
3 | HG02965.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1615-821C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585546 | |||||||
| chr2:241585593 | T | C | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1615-868A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585593 | |||||||
| chr2:241585598 | G | A | 1 | a0002c0003t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1615-873C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585598 | |||||||
| chr2:241585625 | C | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-900G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585625 | |||||||
| chr2:241585641 | C | T | 13 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
13 | HG01981.hp1 HG02074.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1615-916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585641 | |||||||
| chr2:241585647 | G | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0223 a0001c0001t0001g0226 others(5): Show |
9 | HG00735.hp2 HG01081.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-922C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585647 | |||||||
| chr2:241585748 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0358 |
3 | HG02976.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1615-1023T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585748 | |||||||
| chr2:241585806 | G | A | 1 | a0002c0004t0001g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1615-1081C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585806 | |||||||
| chr2:241585912 | C | CA | 27 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0040 others(24): Show |
29 | HG00642.hp2 HG01109.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1615-1188dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(5): Show |
3 | a0001c0002t0001g0303 a0001c0002t0001g0317 a0001c0002t0001g0332 |
3 | HG03490.hp2 NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1615-1199_1615-118 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(6): Show |
17 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0002t0001g0276 others(14): Show |
17 | HG00408.hp1 HG01993.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1615-1200_1615-118 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(7): Show |
19 | a0001c0001t0001g0144 a0001c0002t0001g0025 a0001c0002t0001g0281 others(16): Show |
19 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-1201_1615-118 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(8): Show |
15 | a0001c0002t0001g0198 a0001c0002t0001g0282 a0001c0002t0001g0285 others(12): Show |
15 | HG00438.hp2 HG00639.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1615-1202_1615-118 others(19): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(9): Show |
10 | a0001c0002t0001g0024 a0001c0002t0001g0283 a0001c0002t0001g0284 others(7): Show |
10 | HG00558.hp1 HG01952.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1615-1203_1615-118 others(20): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(10): Show |
5 | a0001c0002t0001g0104 a0001c0002t0001g0286 a0001c0002t0001g0334 others(2): Show |
5 | HG01175.hp2 HG01891.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-1204_1615-118 others(21): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(11): Show |
4 | a0001c0002t0001g0287 a0001c0002t0001g0293 a0001c0002t0001g0336 others(1): Show |
4 | HG00673.hp1 HG01346.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(22): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(12): Show |
5 | a0001c0002t0001g0299 a0001c0002t0001g0301 a0001c0002t0001g0304 others(2): Show |
5 | HG00099.hp2 NA18943.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(23): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(13): Show |
3 | a0001c0002t0001g0302 a0001c0002t0001g0346 a0001c0002t0001g0351 |
3 | HG02080.hp1 HG03017.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(24): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(14): Show |
1 | a0002c0004t0001g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1615-1188_1615-118 others(25): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(15): Show |
2 | a0001c0002t0001g0295 a0001c0002t0001g0300 |
2 | HG03831.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1615-1188_1615-118 others(26): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585912 | C | CAAAAAAA others(19): Show |
1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1615-1188_1615-118 others(30): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585912 | |||||||
| chr2:241585929 | AG | A | 7 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG02897.hp1 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-1205delC | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585929 | |||||||
| chr2:241585930 | G | A | 129 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(126): Show |
134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1615-1205C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585930 | |||||||
| chr2:241585931 | A | G | 1 | a0001c0002t0001g0105 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1615-1206T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585931 | |||||||
| chr2:241585935 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0355 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1615-1211_1615-121 others(20): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585935 | |||||||
| chr2:241585937 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1615-1212T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585937 | |||||||
| chr2:241585940 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0001g0324 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1615-1216_1615-121 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585940 | |||||||
| chr2:241585994 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0001g0358 |
3 | HG02976.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1615-1269C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241585994 | |||||||
| chr2:241586026 | C | T | 1 | a0002c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1615-1301G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586026 | |||||||
| chr2:241586114 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-1389C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586114 | |||||||
| chr2:241586243 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-1518G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586243 | |||||||
| chr2:241586259 | GA | G | 3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-1535delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586259 | |||||||
| chr2:241586262 | G | GA | 46 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(43): Show |
48 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1615-1538dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586262 | |||||||
| chr2:241586262 | GA | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(82): Show |
96 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1615-1538delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586262 | |||||||
| chr2:241586263 | A | G | 3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-1538T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586263 | |||||||
| chr2:241586363 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1615-1638C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586363 | |||||||
| chr2:241586399 | T | G | 1 | a0002c0003t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-1674A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586399 | |||||||
| chr2:241586447 | G | A | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-1722C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586447 | |||||||
| chr2:241586581 | C | T | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1615-1856G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586581 | |||||||
| chr2:241586690 | C | T | 2 | a0001c0002t0001g0330 a0001c0002t0001g0338 |
2 | HG00438.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1615-1965G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586690 | |||||||
| chr2:241586755 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-2030C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586755 | |||||||
| chr2:241586847 | A | G | 2 | a0001c0002t0001g0208 a0001c0002t0001g0209 |
2 | HG00642.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1615-2122T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586847 | |||||||
| chr2:241586874 | C | A | 1 | a0002c0005t0001g0155 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1615-2149G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586874 | |||||||
| chr2:241586902 | T | G | 1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-2177A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586902 | |||||||
| chr2:241586917 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1615-2192T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241586917 | |||||||
| chr2:241587109 | G | A | 1 | a0001c0002t0001g0333 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1615-2384C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587109 | |||||||
| chr2:241587341 | C | T | 1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-2616G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587341 | |||||||
| chr2:241587499 | T | C | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-2774A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587499 | |||||||
| chr2:241587534 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-2809G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587534 | |||||||
| chr2:241587582 | G | A | 1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1615-2857C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587582 | |||||||
| chr2:241587665 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 |
3 | HG01106.hp1 HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1615-2940G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587665 | |||||||
| chr2:241587761 | C | T | 2 | a0001c0002t0001g0325 a0001c0002t0001g0340 |
2 | NA18974.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1615-3036G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587761 | |||||||
| chr2:241587764 | A | T | 16 | a0001c0002t0001g0003 a0001c0002t0001g0203 a0001c0002t0001g0204 others(13): Show |
18 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1615-3039T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587764 | |||||||
| chr2:241587772 | G | A | 1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1615-3047C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587772 | |||||||
| chr2:241587868 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1615-3143A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241587868 | |||||||
| chr2:241588001 | AAGTAAAA others(32): Show |
A | 1 | a0001c0002t0001g0352 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1615-3315_1615-327 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588001 | |||||||
| chr2:241588004 | T | A | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(356): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1615-3279A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588004 | |||||||
| chr2:241588033 | A | G | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-3308T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588033 | |||||||
| chr2:241588162 | C | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1615-3437G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588162 | |||||||
| chr2:241588174 | G | A | 1 | a0002c0003t0001g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1615-3449C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588174 | |||||||
| chr2:241588647 | C | T | 1 | a0001c0002t0001g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1615-3922G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588647 | |||||||
| chr2:241588711 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-3986C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588711 | |||||||
| chr2:241588738 | A | G | 1 | a0002c0003t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-4013T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241588738 | |||||||
| chr2:241589001 | C | T | 1 | a0005c0010t0001g0034 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1615-4276G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589001 | |||||||
| chr2:241589015 | C | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-4290G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589015 | |||||||
| chr2:241589015 | C | G | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1615-4290G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589015 | |||||||
| chr2:241589076 | G | T | 1 | a0002c0004t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1615-4351C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589076 | |||||||
| chr2:241589212 | C | CA | 110 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0001t0001g0143 others(107): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1615-4488dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | |||||||
| chr2:241589212 | C | CAA | 6 | a0001c0002t0001g0024 a0001c0002t0001g0282 a0001c0002t0001g0284 others(3): Show |
6 | HG00639.hp1 HG01346.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615-4489_1615-448 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | |||||||
| chr2:241589212 | C | CAAA | 8 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(5): Show |
8 | HG01175.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-4490_1615-448 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589212 | |||||||
| chr2:241589225 | G | A | 139 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(136): Show |
144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1615-4500C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589225 | |||||||
| chr2:241589366 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1615-4641C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589366 | |||||||
| chr2:241589384 | T | C | 1 | a0002c0003t0001g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1615-4659A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589384 | |||||||
| chr2:241589582 | T | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1615-4857A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589582 | |||||||
| chr2:241589664 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01516.hp1 HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1615-4939C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589664 | |||||||
| chr2:241589681 | T | C | 1 | a0006c0007t0001g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1615-4956A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589681 | |||||||
| chr2:241589695 | G | GA | 143 | a0001c0001t0001g0044 a0001c0001t0001g0061 a0001c0001t0001g0138 others(140): Show |
148 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1615-4971dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241589695 | |||||||
| chr2:241590012 | T | TCAGAGCT others(32): Show |
1 | a0001c0002t0001g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1615-5288_1615-528 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590012 | |||||||
| chr2:241590012 | TCAGAGCT others(32): Show |
T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-5326_1615-528 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590012 | |||||||
| chr2:241590036 | C | T | 139 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(136): Show |
144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1615-5311G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590036 | |||||||
| chr2:241590037 | G | A | 1 | a0002c0003t0001g0257 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1615-5312C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590037 | |||||||
| chr2:241590070 | G | A | 3 | a0001c0001t0001g0061 a0001c0002t0001g0199 a0001c0002t0001g0200 |
3 | HG02622.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-5345C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590070 | |||||||
| chr2:241590089 | C | T | 1 | a0002c0003t0002g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1615-5364G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590089 | |||||||
| chr2:241590102 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-5377C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590102 | |||||||
| chr2:241590151 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1615-5426T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590151 | |||||||
| chr2:241590332 | C | T | 45 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(42): Show |
50 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1615-5607G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590332 | |||||||
| chr2:241590339 | A | ATGATGAG others(146): Show |
1 | a0002c0003t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1615-5615_1615-561 others(157): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590339 | |||||||
| chr2:241590357 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1615-5632T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590357 | |||||||
| chr2:241590366 | A | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5641T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590366 | |||||||
| chr2:241590385 | G | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5660C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590385 | |||||||
| chr2:241590400 | T | A | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5675A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590400 | |||||||
| chr2:241590410 | T | TCGGCTGA others(2018): Show |
1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5686_1615-568 others(2029): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590410 | |||||||
| chr2:241590411 | C | T | 3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1615-5686G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590411 | |||||||
| chr2:241590422 | A | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-5697T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590422 | |||||||
| chr2:241590439 | G | A | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5714C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | |||||||
| chr2:241590439 | G | GCAGAGCT others(1280): Show |
1 | a0002c0004t0001g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5715_1615-571 others(1291): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | |||||||
| chr2:241590439 | G | T | 1 | a0001c0001t0001g0360 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1615-5714C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590439 | |||||||
| chr2:241590444 | G | A | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5719C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590444 | |||||||
| chr2:241590449 | T | C | 32 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(29): Show |
36 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1615-5724A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590449 | |||||||
| chr2:241590457 | T | C | 31 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(28): Show |
35 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1615-5732A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590457 | |||||||
| chr2:241590461 | A | G | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-5736T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590461 | |||||||
| chr2:241590472 | G | T | 1 | a0001c0002t0001g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1615-5747C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590472 | |||||||
| chr2:241590488 | T | C | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5763A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590488 | |||||||
| chr2:241590496 | T | C | 1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5771A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590496 | |||||||
| chr2:241590500 | A | G | 41 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(38): Show |
45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-5775T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590500 | |||||||
| chr2:241590517 | A | G | 23 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0203 others(20): Show |
27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5792T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590517 | |||||||
| chr2:241590517 | A | T | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5792T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590517 | |||||||
| chr2:241590522 | G | A | 8 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0002c0003t0001g0177 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5797C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590522 | |||||||
| chr2:241590527 | T | C | 23 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0203 others(20): Show |
27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5802A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590527 | |||||||
| chr2:241590528 | C | T | 8 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0002c0003t0001g0177 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5803G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590528 | |||||||
| chr2:241590531 | C | CTGA | 108 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(105): Show |
109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1615-5809_1615-580 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | |||||||
| chr2:241590531 | C | CTGACGAT others(74): Show |
23 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0203 others(20): Show |
27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5807_1615-580 others(85): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | |||||||
| chr2:241590531 | C | CTGATGAT others(152): Show |
1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5807_1615-580 others(163): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590531 | |||||||
| chr2:241590536 | G | C | 23 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0203 others(20): Show |
27 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1615-5811C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590536 | |||||||
| chr2:241590536 | G | GATC | 8 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0002c0003t0001g0177 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5812_1615-581 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590536 | |||||||
| chr2:241590538 | T | G | 1 | a0002c0004t0001g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5813A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590538 | |||||||
| chr2:241590538 | T | TAATGGGC others(539): Show |
1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5814_1615-581 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590538 | |||||||
| chr2:241590553 | T | A | 2 | a0002c0004t0001g0172 a0002c0004t0003g0160 |
2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1615-5828A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590553 | |||||||
| chr2:241590558 | A | G | 1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5833T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590558 | |||||||
| chr2:241590563 | C | T | 1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5838G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590563 | |||||||
| chr2:241590567 | CTGA | C | 92 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1615-5845_1615-584 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590567 | |||||||
| chr2:241590577 | G | T | 1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1615-5852C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590577 | |||||||
| chr2:241590592 | T | TCAGAACT others(305): Show |
1 | a0002c0004t0001g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5868_1615-586 others(316): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590592 | |||||||
| chr2:241590602 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
8 | HG01123.hp1 HG01934.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-5877A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590602 | |||||||
| chr2:241590603 | C | T | 1 | a0002c0004t0001g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5878G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590603 | |||||||
| chr2:241590610 | T | C | 9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(6): Show |
9 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-5885A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590610 | |||||||
| chr2:241590614 | G | A | 31 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(28): Show |
35 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1615-5889C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590614 | |||||||
| chr2:241590631 | G | A | 1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5906C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590631 | |||||||
| chr2:241590631 | G | T | 2 | a0002c0004t0001g0172 a0002c0004t0003g0160 |
2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1615-5906C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590631 | |||||||
| chr2:241590641 | C | CCGGCTGA others(1319): Show |
1 | a0002c0003t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1615-5917_1615-591 others(1330): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590641 | |||||||
| chr2:241590641 | C | T | 2 | a0002c0004t0001g0166 a0002c0004t0003g0160 |
2 | HG01123.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1615-5916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590641 | |||||||
| chr2:241590649 | C | CGATAATG others(1550): Show |
3 | a0002c0004t0001g0158 a0002c0006t0001g0156 a0002c0006t0001g0157 |
3 | HG01891.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | |||||||
| chr2:241590649 | C | CGATAATG others(1550): Show |
2 | a0001c0002t0001g0201 a0001c0002t0001g0202 |
2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | |||||||
| chr2:241590649 | C | CGATAATG others(1550): Show |
1 | a0002c0004t0001g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | |||||||
| chr2:241590649 | C | CGATAATG others(1550): Show |
1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1615-5925_1615-592 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | |||||||
| chr2:241590649 | C | T | 2 | a0002c0004t0001g0071 a0002c0004t0003g0160 |
2 | HG01123.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-5924G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590649 | |||||||
| chr2:241590661 | C | CTAGGACA others(1550): Show |
1 | a0002c0004t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590661 | C | CTAGGACA others(1550): Show |
7 | a0001c0002t0001g0003 a0001c0002t0001g0204 a0001c0002t0001g0206 others(4): Show |
9 | HG00423.hp2 HG00544.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590661 | C | CTAGGACA others(1550): Show |
10 | a0001c0002t0001g0004 a0001c0002t0001g0208 a0001c0002t0001g0209 others(7): Show |
12 | HG00642.hp2 HG00741.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1561): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590661 | C | CTAGGACA others(1549): Show |
5 | a0001c0002t0001g0203 a0001c0002t0001g0205 a0001c0002t0001g0207 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-5937_1615-593 others(1560): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590661 | C | CTAGGACA others(305): Show |
1 | a0002c0004t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1615-5937_1615-593 others(316): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590661 | C | G | 8 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0002c0003t0001g0177 others(5): Show |
8 | HG01891.hp2 HG01934.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-5936G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590661 | |||||||
| chr2:241590682 | G | A | 32 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(29): Show |
36 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1615-5957C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590682 | G | GGCTGATG others(539): Show |
1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590682 | G | GGCTGATG others(1319): Show |
1 | a0001c0001t0001g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(1330): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590682 | G | GGCTGATG others(1709): Show |
6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-5958_1615-595 others(1720): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590682 | G | GGCTGATG others(1709): Show |
1 | a0002c0003t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(1720): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590682 | G | GGCTGATG others(32): Show |
1 | a0002c0004t0001g0172 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-5958_1615-595 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590682 | |||||||
| chr2:241590720 | T | C | 1 | a0002c0003t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1615-5995A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590720 | |||||||
| chr2:241590748 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1615-6023A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590748 | |||||||
| chr2:241590753 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1615-6028T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590753 | |||||||
| chr2:241590797 | T | C | 43 | a0001c0001t0001g0135 a0001c0001t0001g0212 a0001c0001t0001g0213 others(40): Show |
47 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1615-6072A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590797 | |||||||
| chr2:241590826 | G | GCAGAGCT others(1046): Show |
1 | a0001c0002t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(1057): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(851): Show |
1 | a0002c0004t0003g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(890): Show |
1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(890): Show |
4 | a0002c0004t0001g0158 a0002c0004t0001g0162 a0002c0006t0001g0156 others(1): Show |
4 | HG01891.hp2 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(890): Show |
1 | a0001c0002t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(890): Show |
24 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0202 others(21): Show |
28 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(901): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590826 | G | GCAGAGCT others(851): Show |
7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-6102_1615-610 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590826 | |||||||
| chr2:241590836 | C | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0002t0001g0206 others(1): Show |
4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6111G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590836 | |||||||
| chr2:241590844 | C | T | 42 | a0001c0001t0001g0135 a0001c0001t0001g0212 a0001c0001t0001g0213 others(39): Show |
46 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1615-6119G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590844 | |||||||
| chr2:241590848 | A | G | 39 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(36): Show |
43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1615-6123T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590848 | |||||||
| chr2:241590856 | C | CTAGGACA others(851): Show |
1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6132_1615-613 others(862): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590856 | |||||||
| chr2:241590865 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
6 | HG01934.hp2 NA18939.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615-6140T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590865 | |||||||
| chr2:241590865 | A | T | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6140T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590865 | |||||||
| chr2:241590870 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6145T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590870 | |||||||
| chr2:241590875 | C | CCGGCTGA others(3812): Show |
1 | a0001c0002t0001g0316 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1615-6151_1615-615 others(3823): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | |||||||
| chr2:241590875 | C | CCGGCTGA others(3815): Show |
1 | a0001c0002t0001g0285 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1615-6151_1615-615 others(3826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | |||||||
| chr2:241590875 | C | T | 39 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(36): Show |
43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1615-6150G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590875 | |||||||
| chr2:241590883 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6158G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590883 | |||||||
| chr2:241590904 | A | G | 1 | a0001c0002t0001g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1615-6179T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590904 | |||||||
| chr2:241590904 | A | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0002c0003t0001g0177 |
3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6179T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590904 | |||||||
| chr2:241590909 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0002c0003t0001g0177 |
3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6184T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590909 | |||||||
| chr2:241590914 | C | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0002t0001g0206 others(1): Show |
4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6189G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590914 | |||||||
| chr2:241590915 | C | T | 1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6190G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590915 | |||||||
| chr2:241590922 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
9 | HG00408.hp2 HG00735.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-6197G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590922 | |||||||
| chr2:241590926 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0002c0003t0001g0177 |
3 | HG00408.hp2 HG01109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1615-6201C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590926 | |||||||
| chr2:241590943 | A | T | 41 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(38): Show |
45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-6218T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590943 | |||||||
| chr2:241590948 | G | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0002t0001g0206 others(1): Show |
4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6223C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590948 | |||||||
| chr2:241590953 | T | C | 4 | a0001c0001t0001g0135 a0001c0001t0001g0238 a0001c0002t0001g0206 others(1): Show |
4 | HG00408.hp2 HG01109.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-6228A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
7 | HG01099.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1475): Show |
1 | a0001c0001t0001g0224 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1486): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0124 others(43): Show |
52 | HG00733.hp2 HG00735.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0002g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1475): Show |
1 | a0001c0001t0001g0232 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1486): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1511): Show |
1 | a0002c0003t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1522): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
35 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0038 others(32): Show |
37 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(2837): Show |
2 | a0002c0003t0001g0099 a0002c0003t0001g0103 |
2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(2848): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
7 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
50 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(47): Show |
54 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1512): Show |
1 | a0001c0001t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1523): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1436): Show |
1 | a0001c0001t0001g0063 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1447): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
11 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(2879): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(2890): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0027 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0002g0050 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0026 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(7): Show |
10 | HG02293.hp1 NA18953.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(14): Show |
19 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1316): Show |
1 | a0002c0003t0001g0023 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1327): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0001c0001t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1553): Show |
1 | a0002c0004t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1564): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590953 | T | TCGGCTGA others(1514): Show |
1 | a0002c0003t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1615-6229_1615-622 others(1525): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590953 | |||||||
| chr2:241590982 | T | A | 41 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(38): Show |
45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1615-6257A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4283): Show |
1 | a0002c0004t0001g0280 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4294): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(1358): Show |
1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(1369): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(1589): Show |
2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(1600): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0347 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4241): Show |
1 | a0001c0002t0001g0313 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4252): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3659): Show |
7 | a0001c0002t0001g0289 a0001c0002t0001g0298 a0001c0002t0001g0299 others(4): Show |
7 | HG00099.hp2 HG03017.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3670): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02257.hp2 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3815): Show |
1 | a0001c0002t0001g0296 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
2 | a0002c0004t0001g0020 a0002c0004t0001g0279 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0325 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0327 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
17 | a0001c0002t0001g0314 a0001c0002t0001g0317 a0001c0002t0001g0318 others(14): Show |
17 | HG00438.hp2 HG01928.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4205): Show |
3 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 |
3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4216): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(2099): Show |
3 | a0001c0002t0001g0292 a0001c0002t0001g0293 a0001c0002t0001g0304 |
3 | HG00558.hp1 HG00673.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(2110): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(6815): Show |
1 | a0002c0004t0001g0277 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(6826): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
10 | a0001c0002t0001g0025 a0001c0002t0001g0291 a0001c0002t0001g0303 others(7): Show |
10 | HG00408.hp1 NA18944.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
2 | a0001c0002t0001g0305 a0001c0002t0001g0319 |
2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
11 | a0001c0002t0001g0281 a0001c0002t0001g0284 a0001c0002t0001g0287 others(8): Show |
11 | HG01346.hp2 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3698): Show |
1 | a0001c0002t0001g0346 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3709): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0342 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4241): Show |
2 | a0001c0002t0001g0343 a0001c0002t0001g0344 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(4252): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
1 | a0001c0002t0001g0352 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3737): Show |
2 | a0001c0002t0001g0351 a0001c0002t0001g0353 |
2 | NA18948.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3748): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3776): Show |
4 | a0001c0002t0001g0286 a0001c0002t0001g0354 a0001c0002t0001g0355 others(1): Show |
4 | HG01175.hp2 NA18939.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-6258_1615-625 others(3787): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(3737): Show |
1 | a0001c0002t0001g0357 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(3748): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4244): Show |
1 | a0001c0002t0001g0333 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4255): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(4205): Show |
1 | a0001c0002t0001g0323 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(4216): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590982 | T | TCAGAGCT others(2528): Show |
1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1615-6258_1615-625 others(2539): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590982 | |||||||
| chr2:241590992 | T | TTGGCTGA others(2138): Show |
1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6268_1615-626 others(2149): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | |||||||
| chr2:241590992 | T | TTGGCTGA others(2021): Show |
1 | a0001c0001t0001g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1615-6268_1615-626 others(2032): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | |||||||
| chr2:241590992 | T | TTGGCTGA others(2177): Show |
2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-6268_1615-626 others(2188): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | |||||||
| chr2:241590992 | T | TTGGCTGA others(2021): Show |
2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6268_1615-626 others(2032): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241590992 | |||||||
| chr2:241591000 | C | T | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6275G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591000 | |||||||
| chr2:241591001 | A | G | 177 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(174): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1615-6276T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591001 | |||||||
| chr2:241591004 | A | G | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6279T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591004 | |||||||
| chr2:241591026 | A | G | 133 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(130): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1615-6301T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591026 | |||||||
| chr2:241591031 | C | T | 133 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(130): Show |
137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1615-6306G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591031 | |||||||
| chr2:241591042 | T | G | 5 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0002c0004t0001g0074 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-6317A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591042 | |||||||
| chr2:241591060 | T | A | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6335A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591060 | |||||||
| chr2:241591060 | T | G | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-6335A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591060 | |||||||
| chr2:241591074 | CTGA | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0043 others(10): Show |
13 | HG01981.hp1 HG02074.hp1 HG02293.hp1 others(10): Show |
intron_variant | MODIFIER | c.1615-6352_1615-635 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591074 | |||||||
| chr2:241591078 | T | C | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6353A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591078 | |||||||
| chr2:241591082 | G | A | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6357C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591082 | |||||||
| chr2:241591098 | G | C | 142 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(139): Show |
147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1615-6373C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591098 | |||||||
| chr2:241591099 | A | T | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6374T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591099 | |||||||
| chr2:241591104 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6379T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591104 | |||||||
| chr2:241591109 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6384G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591109 | |||||||
| chr2:241591110 | A | C | 142 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(139): Show |
147 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1615-6385T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591110 | |||||||
| chr2:241591138 | T | A | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6413A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(110): Show |
1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6414_1615-641 others(121): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(539): Show |
2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(500): Show |
1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1615-6414_1615-641 others(511): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(539): Show |
2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(539): Show |
3 | a0001c0001t0001g0061 a0002c0005t0001g0154 a0002c0005t0001g0155 |
3 | HG02622.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(550): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591138 | T | TCAGAGCT others(32): Show |
132 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(129): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1615-6414_1615-641 others(43): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591138 | |||||||
| chr2:241591148 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1615-6423G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591148 | |||||||
| chr2:241591149 | C | A | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6424G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591149 | |||||||
| chr2:241591155 | A | G | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1615-6430T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591155 | |||||||
| chr2:241591163 | G | C | 1 | a0001c0002t0001g0303 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1615-6438C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591163 | |||||||
| chr2:241591182 | G | A | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6457C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591182 | |||||||
| chr2:241591187 | T | C | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6462A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591187 | |||||||
| chr2:241591195 | T | C | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6470A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591195 | |||||||
| chr2:241591204 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1615-6479C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591204 | |||||||
| chr2:241591220 | A | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1615-6495T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591220 | |||||||
| chr2:241591221 | A | G | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1615-6496T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591221 | |||||||
| chr2:241591231 | T | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-6506A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591231 | |||||||
| chr2:241591250 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1615-6525C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591250 | |||||||
| chr2:241591420 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-6695G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591420 | |||||||
| chr2:241591461 | T | C | 1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1615-6736A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591461 | |||||||
| chr2:241591614 | T | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-6889A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591614 | |||||||
| chr2:241591718 | G | A | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1615-6993C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591718 | |||||||
| chr2:241591749 | A | T | 1 | a0002c0003t0001g0196 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1615-7024T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591749 | |||||||
| chr2:241591821 | G | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-7096C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591821 | |||||||
| chr2:241591879 | C | G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1615-7154G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241591879 | |||||||
| chr2:241592062 | C | T | 2 | a0001c0002t0001g0294 a0001c0002t0001g0295 |
2 | NA19006.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1615-7337G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592062 | |||||||
| chr2:241592107 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1615-7382C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592107 | |||||||
| chr2:241592184 | G | A | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1615-7459C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592184 | |||||||
| chr2:241592250 | G | A | 98 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(95): Show |
98 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1615-7525C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592250 | |||||||
| chr2:241592257 | T | C | 3 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 |
3 | NA18992.hp2 NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1615-7532A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592257 | |||||||
| chr2:241592333 | C | T | 1 | a0002c0003t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1615-7608G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592333 | |||||||
| chr2:241592370 | C | T | 1 | a0002c0003t0001g0173 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1615-7645G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592370 | |||||||
| chr2:241592557 | C | T | 1 | a0001c0002t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1615-7832G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592557 | |||||||
| chr2:241592567 | G | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1615-7842C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592567 | |||||||
| chr2:241592726 | G | A | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18979.hp2 NA19010.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1615-8001C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592726 | |||||||
| chr2:241592774 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1615-8049G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241592774 | |||||||
| chr2:241593014 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1615-8289C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593014 | |||||||
| chr2:241593078 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-8353A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593078 | |||||||
| chr2:241593289 | G | A | 4 | a0002c0003t0001g0190 a0002c0003t0001g0191 a0002c0003t0001g0192 others(1): Show |
4 | NA18945.hp2 NA18969.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-8564C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593289 | |||||||
| chr2:241593337 | C | G | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+8559G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593337 | |||||||
| chr2:241593355 | C | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+8541G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593355 | |||||||
| chr2:241593373 | T | G | 17 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(14): Show |
18 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1614+8523A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593373 | |||||||
| chr2:241593500 | C | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+8396G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593500 | |||||||
| chr2:241593573 | TA | T | 49 | a0001c0001t0001g0061 a0001c0001t0001g0212 a0001c0001t0001g0213 others(46): Show |
54 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1614+8322delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593573 | |||||||
| chr2:241593593 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+8303C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593593 | |||||||
| chr2:241593630 | T | G | 2 | a0001c0002t0001g0320 a0001c0002t0001g0337 |
2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.1614+8266A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593630 | |||||||
| chr2:241593633 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+8263T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593633 | |||||||
| chr2:241593635 | G | C | 1 | a0001c0001t0001g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+8261C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593635 | |||||||
| chr2:241593964 | T | C | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1614+7932A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241593964 | |||||||
| chr2:241594150 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1614+7746C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594150 | |||||||
| chr2:241594229 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+7667C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594229 | |||||||
| chr2:241594230 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+7666A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594230 | |||||||
| chr2:241594281 | T | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+7615A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594281 | |||||||
| chr2:241594615 | G | A | 2 | a0002c0004t0001g0158 a0002c0004t0001g0162 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1614+7281C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594615 | |||||||
| chr2:241594721 | G | A | 3 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0002c0004t0001g0171 |
3 | HG00642.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1614+7175C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594721 | |||||||
| chr2:241594818 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
105 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1614+7078G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594818 | |||||||
| chr2:241594826 | C | T | 3 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 |
3 | HG02559.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1614+7070G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594826 | |||||||
| chr2:241594855 | T | C | 1 | a0001c0002t0001g0316 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1614+7041A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594855 | |||||||
| chr2:241594992 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6904C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241594992 | |||||||
| chr2:241595003 | T | C | 2 | a0001c0002t0001g0317 a0001c0002t0001g0318 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1614+6893A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595003 | |||||||
| chr2:241595045 | G | A | 1 | a0002c0003t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1614+6851C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595045 | |||||||
| chr2:241595052 | C | T | 131 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(128): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1614+6844G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595052 | |||||||
| chr2:241595234 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1614+6662G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595234 | |||||||
| chr2:241595294 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6602G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595294 | |||||||
| chr2:241595314 | C | T | 1 | a0002c0003t0001g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1614+6582G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595314 | |||||||
| chr2:241595333 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1614+6563C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595333 | |||||||
| chr2:241595366 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1614+6530T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595366 | |||||||
| chr2:241595399 | A | G | 2 | a0001c0002t0001g0292 a0001c0002t0001g0293 |
2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.1614+6497T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595399 | |||||||
| chr2:241595412 | C | T | 1 | a0002c0003t0002g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1614+6484G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595412 | |||||||
| chr2:241595551 | C | T | 3 | a0001c0002t0001g0201 a0001c0002t0001g0202 a0002c0003t0001g0092 |
3 | HG01261.hp1 HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1614+6345G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595551 | |||||||
| chr2:241595594 | G | A | 1 | a0002c0003t0001g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+6302C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595594 | |||||||
| chr2:241595650 | G | A | 140 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+6246C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595650 | |||||||
| chr2:241595652 | A | G | 1 | a0002c0004t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1614+6244T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595652 | |||||||
| chr2:241595717 | C | G | 1 | a0002c0003t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1614+6179G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595717 | |||||||
| chr2:241595772 | G | A | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+6124C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595772 | |||||||
| chr2:241595783 | C | A | 1 | a0002c0003t0001g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1614+6113G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595783 | |||||||
| chr2:241595859 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+6037C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595859 | |||||||
| chr2:241595922 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1614+5974A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595922 | |||||||
| chr2:241595962 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+5934G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595962 | |||||||
| chr2:241595970 | G | A | 28 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(25): Show |
32 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1614+5926C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595970 | |||||||
| chr2:241595990 | A | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1614+5906T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241595990 | |||||||
| chr2:241596009 | G | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+5887C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596009 | |||||||
| chr2:241596092 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+5804G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596092 | |||||||
| chr2:241596148 | A | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0211 |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+5748T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596148 | |||||||
| chr2:241596163 | A | ATT | 44 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
48 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1614+5732_1614+573 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596163 | |||||||
| chr2:241596166 | A | T | 44 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
48 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1614+5730T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596166 | |||||||
| chr2:241596228 | G | A | 1 | a0002c0004t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1614+5668C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596228 | |||||||
| chr2:241596336 | G | A | 141 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(138): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.1614+5560C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596336 | |||||||
| chr2:241596456 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1614+5440C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596456 | |||||||
| chr2:241596508 | C | CA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0037 others(19): Show |
24 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+5387dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | |||||||
| chr2:241596508 | CA | C | 92 | a0001c0001t0001g0061 a0001c0001t0001g0142 a0001c0001t0001g0143 others(89): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1614+5387delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | |||||||
| chr2:241596508 | CAA | C | 48 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0104 others(45): Show |
48 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1614+5386_1614+538 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596508 | |||||||
| chr2:241596520 | A | G | 1 | a0002c0003t0001g0185 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1614+5376T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596520 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
1 | a0001c0001t0001g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
1 | a0001c0002t0001g0120 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1975): Show |
1 | a0001c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1986): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
11 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
11 | HG01981.hp1 HG02293.hp1 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0032 others(1): Show |
4 | HG00621.hp2 NA18941.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
16 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(13): Show |
18 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
1 | a0001c0001t0001g0055 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 |
3 | HG01106.hp1 HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
9 | a0001c0001t0001g0028 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00597.hp1 HG02027.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
104 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(101): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
1 | a0001c0002t0001g0123 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
1 | a0003c0008t0001g0073 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
1 | a0002c0003t0001g0094 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
7 | a0001c0002t0001g0310 a0001c0002t0001g0311 a0001c0002t0001g0312 others(4): Show |
7 | HG00438.hp2 HG01891.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
113 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(110): Show |
118 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1930): Show |
3 | a0001c0002t0001g0289 a0001c0002t0001g0308 a0001c0002t0001g0327 |
3 | HG03491.hp2 NA18942.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1933): Show |
1 | a0002c0004t0003g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1944): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1927): Show |
1 | a0002c0004t0003g0163 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1938): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
3 | a0002c0004t0003g0159 a0002c0004t0003g0160 a0002c0004t0003g0161 |
3 | HG01081.hp1 HG01123.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1931): Show |
1 | a0001c0002t0001g0336 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1930): Show |
1 | a0002c0004t0001g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1932): Show |
1 | a0001c0001t0001g0061 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1943): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1930): Show |
7 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596529 | G | GGGCGCGG others(1930): Show |
1 | a0001c0001t0001g0213 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1614+5366_1614+536 others(1941): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596529 | |||||||
| chr2:241596531 | G | GCGCGGTG others(1931): Show |
1 | a0001c0002t0001g0286 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1614+5364_1614+536 others(1942): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596531 | |||||||
| chr2:241596537 | T | C | 1 | a0001c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1614+5359A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596537 | |||||||
| chr2:241596579 | C | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1614+5317G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596579 | |||||||
| chr2:241596623 | G | A | 1 | a0001c0002t0001g0025 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1614+5273C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596623 | |||||||
| chr2:241596653 | G | T | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+5243C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596653 | |||||||
| chr2:241596759 | C | T | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+5137G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596759 | |||||||
| chr2:241596801 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0246 a0001c0001t0001g0248 others(2): Show |
7 | HG00558.hp2 NA18612.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.1614+5095C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596801 | |||||||
| chr2:241596892 | G | C | 1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1614+5004C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241596892 | |||||||
| chr2:241597027 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1614+4869G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597027 | |||||||
| chr2:241597170 | G | A | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+4726C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597170 | |||||||
| chr2:241597236 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1614+4660G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597236 | |||||||
| chr2:241597426 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0002c0003t0001g0102 |
3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1614+4470C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597426 | |||||||
| chr2:241597483 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1614+4413T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597483 | |||||||
| chr2:241597533 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+4363G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597533 | |||||||
| chr2:241597568 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1614+4328A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597568 | |||||||
| chr2:241597717 | G | A | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+4179C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597717 | |||||||
| chr2:241597926 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+3970C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597926 | |||||||
| chr2:241597978 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1614+3918G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | |||||||
| chr2:241597978 | CA | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1614+3917delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | |||||||
| chr2:241597978 | CAA | C | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
141 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.1614+3916_1614+391 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241597978 | |||||||
| chr2:241598004 | A | G | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+3892T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598004 | |||||||
| chr2:241598007 | A | T | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+3889T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598007 | |||||||
| chr2:241598277 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+3619G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598277 | |||||||
| chr2:241598291 | G | A | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1614+3605C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598291 | |||||||
| chr2:241598415 | TC | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+3480delG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598415 | |||||||
| chr2:241598421 | A | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
5 | HG00597.hp2 HG00621.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+3475T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598421 | |||||||
| chr2:241598453 | T | G | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+3443A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598453 | |||||||
| chr2:241598518 | A | AT | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0002c0003t0001g0263 |
3 | HG01099.hp2 HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1614+3377dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598518 | |||||||
| chr2:241598647 | T | G | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+3249A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598647 | |||||||
| chr2:241598735 | C | T | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1614+3161G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598735 | |||||||
| chr2:241598860 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3036A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598860 | |||||||
| chr2:241598875 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3021G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598875 | |||||||
| chr2:241598876 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1614+3020A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598876 | |||||||
| chr2:241598907 | G | A | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+2989C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598907 | |||||||
| chr2:241598912 | G | A | 6 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
6 | HG00735.hp1 HG01123.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+2984C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598912 | |||||||
| chr2:241598924 | GA | G | 139 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(136): Show |
144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1614+2971delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241598924 | |||||||
| chr2:241599060 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0127 a0001c0001t0001g0128 |
4 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2836A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599060 | |||||||
| chr2:241599081 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1614+2815T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599081 | |||||||
| chr2:241599129 | G | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2767C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599129 | |||||||
| chr2:241599183 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+2713G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599183 | |||||||
| chr2:241599206 | C | T | 4 | a0001c0002t0001g0314 a0001c0002t0001g0317 a0001c0002t0001g0318 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2690G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599206 | |||||||
| chr2:241599251 | C | CA | 108 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(105): Show |
109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1614+2644dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599251 | |||||||
| chr2:241599251 | C | CAA | 36 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(33): Show |
40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1614+2643_1614+264 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599251 | |||||||
| chr2:241599521 | C | T | 57 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(54): Show |
62 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1614+2375G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599521 | |||||||
| chr2:241599528 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1614+2368T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599528 | |||||||
| chr2:241599532 | A | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0211 |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+2364T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599532 | |||||||
| chr2:241599567 | C | G | 1 | a0001c0002t0001g0317 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1614+2329G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599567 | |||||||
| chr2:241599711 | C | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2185G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599711 | |||||||
| chr2:241599828 | G | C | 2 | a0002c0006t0001g0156 a0002c0006t0001g0157 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1614+2068C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599828 | |||||||
| chr2:241599831 | A | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1614+2065T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599831 | |||||||
| chr2:241599911 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1614+1985G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599911 | |||||||
| chr2:241599930 | C | T | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1614+1966G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599930 | |||||||
| chr2:241599957 | C | G | 1 | a0001c0002t0001g0283 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1614+1939G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599957 | |||||||
| chr2:241599965 | T | G | 1 | a0002c0003t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1614+1931A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241599965 | |||||||
| chr2:241600089 | G | A | 1 | a0001c0002t0001g0313 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1614+1807C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600089 | |||||||
| chr2:241600095 | C | T | 1 | a0001c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1614+1801G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600095 | |||||||
| chr2:241600133 | C | T | 1 | a0001c0002t0001g0322 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1614+1763G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600133 | |||||||
| chr2:241600245 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+1651A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600245 | |||||||
| chr2:241600249 | C | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1614+1647G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600249 | |||||||
| chr2:241600316 | T | C | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+1580A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600316 | |||||||
| chr2:241600531 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+1365A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600531 | |||||||
| chr2:241600555 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1614+1341C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600555 | |||||||
| chr2:241600727 | C | CA | 89 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0127 others(86): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1614+1168dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | |||||||
| chr2:241600727 | C | CAA | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(39): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1614+1167_1614+116 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | |||||||
| chr2:241600727 | C | CAAA | 46 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0146 others(43): Show |
53 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1614+1166_1614+116 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600727 | |||||||
| chr2:241600975 | TA | T | 139 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0143 others(136): Show |
143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1614+920delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600975 | |||||||
| chr2:241600976 | A | T | 1 | a0002c0003t0001g0259 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1614+920T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241600976 | |||||||
| chr2:241601063 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
8 | HG01934.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614+833C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601063 | |||||||
| chr2:241601096 | T | C | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+800A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601096 | |||||||
| chr2:241601138 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1614+758G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601138 | |||||||
| chr2:241601147 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1614+749C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601147 | |||||||
| chr2:241601222 | G | A | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1614+674C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601222 | |||||||
| chr2:241601226 | C | T | 92 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1614+670G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601226 | |||||||
| chr2:241601264 | C | A | 1 | a0001c0002t0001g0304 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1614+632G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601264 | |||||||
| chr2:241601323 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1614+573T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601323 | |||||||
| chr2:241601435 | G | A | 1 | a0001c0002t0001g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1614+461C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601435 | |||||||
| chr2:241601632 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1614+264C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601632 | |||||||
| chr2:241601820 | G | A | 1 | a0001c0002t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1614+76C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601820 | |||||||
| chr2:241601839 | T | C | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+57A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601839 | |||||||
| chr2:241601874 | C | T | 1 | a0002c0004t0003g0160 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1614+22G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 5/5 | chr2 | 241601874 | |||||||
| chr2:241602038 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1511-39G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602038 | |||||||
| chr2:241602058 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1511-59A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602058 | |||||||
| chr2:241602197 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1511-198C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602197 | |||||||
| chr2:241602350 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(64): Show |
73 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1511-351C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602350 | |||||||
| chr2:241602358 | G | GT | 17 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0054 others(14): Show |
17 | HG00438.hp2 HG00544.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-360dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602358 | |||||||
| chr2:241602372 | C | CA | 3 | a0001c0001t0001g0131 a0001c0001t0001g0230 a0002c0003t0001g0184 |
3 | HG00733.hp2 HG01358.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1511-374_1511-373i others(3): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602372 | |||||||
| chr2:241602554 | C | T | 1 | a0002c0003t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1510+416G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602554 | |||||||
| chr2:241602804 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1510+166C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602804 | |||||||
| chr2:241602883 | T | C | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1510+87A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602883 | |||||||
| chr2:241602889 | T | C | 7 | a0001c0002t0001g0003 a0001c0002t0001g0204 a0001c0002t0001g0206 others(4): Show |
9 | HG00423.hp2 HG00544.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510+81A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 4/5 | chr2 | 241602889 | |||||||
| chr2:241603084 | A | T | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.1401-5T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603084 | |||||||
| chr2:241603139 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1401-60G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603139 | |||||||
| chr2:241603259 | T | C | 3 | a0001c0002t0001g0305 a0001c0002t0001g0319 a0002c0004t0001g0277 |
3 | HG03654.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1401-180A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603259 | |||||||
| chr2:241603294 | ACACACCT others(193): Show |
A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0038 others(39): Show |
44 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.1401-415_1401-216d others(2): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603294 | |||||||
| chr2:241603311 | C | T | 2 | a0002c0004t0001g0074 a0002c0004t0001g0077 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1401-232G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603311 | |||||||
| chr2:241603380 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1401-301A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603380 | |||||||
| chr2:241603394 | G | A | 130 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(127): Show |
134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1401-315C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603394 | |||||||
| chr2:241603588 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1401-509A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603588 | |||||||
| chr2:241603775 | C | G | 2 | a0001c0002t0001g0322 a0001c0002t0001g0323 |
2 | NA18982.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1401-696G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603775 | |||||||
| chr2:241603883 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401-804A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603883 | |||||||
| chr2:241603958 | GCTGGGCA others(9): Show |
G | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1401-895_1401-880d others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241603958 | |||||||
| chr2:241604222 | C | T | 2 | a0002c0003t0001g0186 a0002c0003t0001g0197 |
2 | HG02895.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1401-1143G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604222 | |||||||
| chr2:241604236 | A | AATTT | 20 | a0001c0001t0001g0061 a0001c0001t0001g0268 a0001c0001t0001g0269 others(17): Show |
21 | HG02056.hp2 HG02523.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1401-1161_1401-115 others(8): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604236 | |||||||
| chr2:241604375 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1401-1296G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604375 | |||||||
| chr2:241604644 | TAGTGATC others(141): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1400+1522_1401-156 others(4): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604644 | |||||||
| chr2:241604807 | C | G | 1 | a0001c0002t0001g0282 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1400+1507G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241604807 | |||||||
| chr2:241605182 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1400+1132G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605182 | |||||||
| chr2:241605326 | C | T | 1 | a0002c0003t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1400+988G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605326 | |||||||
| chr2:241605330 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1400+984C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605330 | |||||||
| chr2:241605339 | A | G | 3 | a0002c0003t0001g0090 a0002c0003t0001g0093 a0002c0003t0001g0098 |
3 | HG00741.hp2 HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1400+975T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605339 | |||||||
| chr2:241605452 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1400+862A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605452 | |||||||
| chr2:241605510 | A | G | 35 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(32): Show |
40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1400+804T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605510 | |||||||
| chr2:241605547 | A | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1400+767T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605547 | |||||||
| chr2:241605718 | T | A | 1 | a0002c0003t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1400+596A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605718 | |||||||
| chr2:241605722 | C | CT | 42 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(39): Show |
46 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1400+591dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605722 | |||||||
| chr2:241605982 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1400+332C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241605982 | |||||||
| chr2:241606036 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1400+278T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606036 | |||||||
| chr2:241606191 | T | G | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+123A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606191 | |||||||
| chr2:241606192 | A | C | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+122T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606192 | |||||||
| chr2:241606193 | G | A | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+121C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606193 | |||||||
| chr2:241606199 | C | A | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+115G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606199 | |||||||
| chr2:241606202 | G | C | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+112C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606202 | |||||||
| chr2:241606204 | T | C | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+110A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606204 | |||||||
| chr2:241606205 | C | A | 1 | a0001c0002t0004g0364 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1400+109G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606205 | |||||||
| chr2:241606241 | C | A | 1 | a0001c0002t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1400+73G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606241 | |||||||
| chr2:241606301 | G | A | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1400+13C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 3/5 | chr2 | 241606301 | |||||||
| chr2:241606894 | C | A | 41 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(38): Show |
45 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1241-421G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606894 | |||||||
| chr2:241606928 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-455G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606928 | |||||||
| chr2:241606948 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-475G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606948 | |||||||
| chr2:241606980 | CA | C | 15 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(12): Show |
15 | HG02056.hp2 HG02523.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1241-508delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241606980 | |||||||
| chr2:241607007 | G | C | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-534C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607007 | |||||||
| chr2:241607063 | T | A | 1 | a0001c0002t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1241-590A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607063 | |||||||
| chr2:241607372 | G | A | 1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1241-899C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607372 | |||||||
| chr2:241607411 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1241-938C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607411 | |||||||
| chr2:241607467 | G | A | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1241-994C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607467 | |||||||
| chr2:241607471 | G | T | 1 | a0001c0002t0001g0320 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1241-998C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607471 | |||||||
| chr2:241607519 | C | T | 37 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(34): Show |
37 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(34): Show |
intron_variant | MODIFIER | c.1241-1046G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607519 | |||||||
| chr2:241607597 | C | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(32): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-1124G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607597 | |||||||
| chr2:241607645 | C | T | 1 | a0001c0002t0001g0338 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1241-1172G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607645 | |||||||
| chr2:241607672 | G | C | 1 | a0001c0002t0001g0310 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1241-1199C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607672 | |||||||
| chr2:241607673 | C | G | 1 | a0001c0002t0001g0310 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1241-1200G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607673 | |||||||
| chr2:241607685 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-1212C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607685 | |||||||
| chr2:241607689 | G | A | 35 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(32): Show |
40 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-1216C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607689 | |||||||
| chr2:241607691 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1241-1218C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607691 | |||||||
| chr2:241607718 | A | G | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-1245T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607718 | |||||||
| chr2:241607733 | C | CCCCAGTG others(58): Show |
2 | a0001c0001t0001g0131 a0002c0003t0001g0087 |
2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1241-1325_1241-126 others(69): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607733 | |||||||
| chr2:241607887 | G | A | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-1414C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607887 | |||||||
| chr2:241607900 | A | G | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(356): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1241-1427T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607900 | |||||||
| chr2:241607906 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-1433G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607906 | |||||||
| chr2:241607934 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-1461G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607934 | |||||||
| chr2:241607960 | A | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-1487T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241607960 | |||||||
| chr2:241608127 | G | T | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-1654C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608127 | |||||||
| chr2:241608150 | T | C | 1 | a0002c0004t0001g0075 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1241-1677A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608150 | |||||||
| chr2:241608212 | T | G | 1 | a0001c0002t0004g0362 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1241-1739A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608212 | |||||||
| chr2:241608251 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-1778C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608251 | |||||||
| chr2:241608389 | T | C | 1 | a0001c0002t0001g0152 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1241-1916A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608389 | |||||||
| chr2:241608409 | A | G | 3 | a0001c0002t0001g0206 a0001c0002t0001g0341 a0002c0004t0001g0169 |
3 | HG02132.hp1 NA19000.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1241-1936T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608409 | |||||||
| chr2:241608549 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(31): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1241-2076G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608549 | |||||||
| chr2:241608620 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2147A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608620 | |||||||
| chr2:241608690 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2217G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608690 | |||||||
| chr2:241608802 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-2329C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608802 | |||||||
| chr2:241608977 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | NA19070.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1241-2504C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241608977 | |||||||
| chr2:241609293 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-2820C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609293 | |||||||
| chr2:241609343 | G | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-2870C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609343 | |||||||
| chr2:241609425 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA18960.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1241-2952T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609425 | |||||||
| chr2:241609443 | G | A | 3 | a0001c0002t0001g0208 a0001c0002t0001g0209 a0002c0004t0001g0171 |
3 | HG00642.hp2 HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1241-2970C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609443 | |||||||
| chr2:241609483 | T | C | 35 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0002t0001g0003 others(32): Show |
39 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1241-3010A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609483 | |||||||
| chr2:241609543 | T | C | 1 | a0002c0003t0001g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241-3070A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609543 | |||||||
| chr2:241609652 | T | C | 1 | a0001c0002t0001g0348 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1241-3179A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609652 | |||||||
| chr2:241609718 | C | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-3245G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609718 | |||||||
| chr2:241609718 | C | T | 1 | a0001c0002t0001g0013 | 2 | NA18971.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1241-3245G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609718 | |||||||
| chr2:241609772 | G | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-3299C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609772 | |||||||
| chr2:241609782 | C | CA | 134 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(131): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1241-3310dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241609782 | |||||||
| chr2:241610045 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1241-3572C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610045 | |||||||
| chr2:241610068 | G | T | 1 | a0001c0002t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1241-3595C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610068 | |||||||
| chr2:241610139 | A | G | 10 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
10 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1241-3666T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610139 | |||||||
| chr2:241610197 | C | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0057 |
2 | NA18949.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1241-3724G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610197 | |||||||
| chr2:241610209 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1241-3736T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610209 | |||||||
| chr2:241610287 | A | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-3814T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610287 | |||||||
| chr2:241610317 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1241-3844G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610317 | |||||||
| chr2:241610327 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-3854A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610327 | |||||||
| chr2:241610515 | G | C | 1 | a0002c0003t0001g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1241-4042C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610515 | |||||||
| chr2:241610532 | A | G | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-4059T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610532 | |||||||
| chr2:241610534 | C | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-4061G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610534 | |||||||
| chr2:241610553 | G | A | 2 | a0001c0002t0001g0003 a0001c0002t0001g0204 |
4 | HG00423.hp2 HG02135.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-4080C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610553 | |||||||
| chr2:241610620 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1241-4147G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610620 | |||||||
| chr2:241610640 | C | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-4167G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610640 | |||||||
| chr2:241610784 | A | C | 2 | a0002c0003t0001g0099 a0002c0003t0001g0103 |
2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1241-4311T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610784 | |||||||
| chr2:241610869 | TGGGGCCA others(5): Show |
T | 3 | a0001c0001t0001g0275 a0002c0003t0001g0197 a0002c0003t0001g0260 |
3 | HG02895.hp2 HG03491.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1241-4408_1241-439 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610869 | |||||||
| chr2:241610891 | G | A | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1241-4418C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610891 | |||||||
| chr2:241610995 | C | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0230 a0001c0001t0001g0241 others(9): Show |
13 | HG01071.hp2 HG01168.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1241-4522G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241610995 | |||||||
| chr2:241611120 | T | G | 90 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(87): Show |
90 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1241-4647A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611120 | |||||||
| chr2:241611316 | GC | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 |
3 | HG01106.hp1 HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-4844delG | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611316 | |||||||
| chr2:241611399 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1241-4926T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611399 | |||||||
| chr2:241611724 | C | CA | 8 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0146 others(5): Show |
8 | HG01106.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-5252dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611724 | |||||||
| chr2:241611724 | CA | C | 134 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(131): Show |
138 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.1241-5252delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611724 | |||||||
| chr2:241611955 | T | C | 91 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-5482A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611955 | |||||||
| chr2:241611959 | G | A | 91 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-5486C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611959 | |||||||
| chr2:241611971 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5498G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241611971 | |||||||
| chr2:241612097 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-5624G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612097 | |||||||
| chr2:241612117 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5644C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612117 | |||||||
| chr2:241612124 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-5651T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612124 | |||||||
| chr2:241612220 | G | A | 1 | a0002c0004t0001g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241-5747C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612220 | |||||||
| chr2:241612243 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1241-5770C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612243 | |||||||
| chr2:241612279 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0002c0003t0001g0102 |
3 | HG01109.hp2 HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1241-5806C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612279 | |||||||
| chr2:241612304 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-5831C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612304 | |||||||
| chr2:241612309 | C | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-5836G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612309 | |||||||
| chr2:241612329 | G | T | 1 | a0001c0002t0001g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1241-5856C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612329 | |||||||
| chr2:241612429 | C | T | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-5956G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612429 | |||||||
| chr2:241612430 | T | A | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-5957A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612430 | |||||||
| chr2:241612464 | C | T | 1 | a0001c0002t0001g0315 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1241-5991G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612464 | |||||||
| chr2:241612912 | C | T | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1241-6439G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612912 | |||||||
| chr2:241612932 | C | G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-6459G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612932 | |||||||
| chr2:241612964 | T | C | 91 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-6491A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241612964 | |||||||
| chr2:241613274 | C | CA | 9 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0229 others(6): Show |
9 | HG01891.hp1 HG02148.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1241-6802dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613274 | |||||||
| chr2:241613274 | CA | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0212 others(3): Show |
6 | HG02080.hp2 HG02897.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-6802delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613274 | |||||||
| chr2:241613289 | A | G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-6816T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613289 | |||||||
| chr2:241613306 | C | CA | 5 | a0001c0002t0001g0324 a0001c0002t0001g0325 a0001c0002t0001g0326 others(2): Show |
5 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-6834dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613306 | |||||||
| chr2:241613412 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0065 others(1): Show |
5 | HG02145.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-6939T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613412 | |||||||
| chr2:241613635 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1241-7162C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613635 | |||||||
| chr2:241613659 | G | C | 2 | a0001c0002t0001g0201 a0001c0002t0001g0202 |
2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1241-7186C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613659 | |||||||
| chr2:241613775 | A | G | 5 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0002c0004t0001g0074 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-7302T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241613775 | |||||||
| chr2:241614407 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-7934G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614407 | |||||||
| chr2:241614801 | A | G | 1 | a0001c0002t0001g0355 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1241-8328T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614801 | |||||||
| chr2:241614889 | CAAAACA | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0274 a0002c0003t0001g0019 others(1): Show |
5 | HG02559.hp2 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-8422_1241-841 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614889 | |||||||
| chr2:241614889 | CAAAACAA others(5): Show |
C | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-8428_1241-841 others(16): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241614889 | |||||||
| chr2:241615065 | A | G | 1 | a0001c0001t0001g0015 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1241-8592T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615065 | |||||||
| chr2:241615071 | T | C | 1 | a0002c0004t0001g0169 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1241-8598A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615071 | |||||||
| chr2:241615091 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1241-8618G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615091 | |||||||
| chr2:241615101 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1241-8628C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615101 | |||||||
| chr2:241615159 | G | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1241-8686C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615159 | |||||||
| chr2:241615244 | G | A | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1241-8771C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615244 | |||||||
| chr2:241615288 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-8815G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615288 | |||||||
| chr2:241615362 | C | A | 1 | a0001c0002t0001g0106 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1241-8889G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615362 | |||||||
| chr2:241615411 | C | A | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1241-8938G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615411 | |||||||
| chr2:241615497 | C | T | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-9024G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615497 | |||||||
| chr2:241615665 | G | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-9192C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615665 | |||||||
| chr2:241615727 | G | A | 1 | a0001c0002t0001g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1241-9254C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615727 | |||||||
| chr2:241615797 | C | T | 1 | a0002c0003t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1241-9324G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615797 | |||||||
| chr2:241615834 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1241-9361T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615834 | |||||||
| chr2:241615841 | G | A | 2 | a0001c0002t0001g0004 a0001c0002t0001g0211 |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-9368C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615841 | |||||||
| chr2:241615848 | G | A | 1 | a0002c0003t0001g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1241-9375C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615848 | |||||||
| chr2:241615869 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1241-9396C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615869 | |||||||
| chr2:241615881 | C | T | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0351 others(5): Show |
8 | HG02074.hp1 NA18939.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241-9408G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615881 | |||||||
| chr2:241615901 | G | A | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-9428C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615901 | |||||||
| chr2:241615987 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1241-9514T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615987 | |||||||
| chr2:241615993 | C | T | 4 | a0002c0003t0001g0081 a0002c0003t0001g0082 a0002c0003t0001g0089 others(1): Show |
4 | HG00733.hp1 HG01993.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-9520G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241615993 | |||||||
| chr2:241616038 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-9565C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616038 | |||||||
| chr2:241616165 | T | C | 2 | a0002c0004t0001g0020 a0002c0004t0001g0279 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1241-9692A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616165 | |||||||
| chr2:241616182 | C | T | 1 | a0001c0002t0001g0119 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1241-9709G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616182 | |||||||
| chr2:241616183 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1241-9710C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616183 | |||||||
| chr2:241616281 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1241-9808T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616281 | |||||||
| chr2:241616654 | A | T | 1 | a0001c0001t0002g0049 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1241-10181T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616654 | |||||||
| chr2:241616722 | T | A | 1 | a0002c0003t0001g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1241-10249A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616722 | |||||||
| chr2:241616746 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1241-10273G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616746 | |||||||
| chr2:241616882 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-10409C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616882 | |||||||
| chr2:241616926 | A | G | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1241-10453T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616926 | |||||||
| chr2:241616991 | C | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-10518G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241616991 | |||||||
| chr2:241617000 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0238 |
3 | HG01106.hp1 HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1241-10527G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617000 | |||||||
| chr2:241617114 | A | G | 5 | a0001c0002t0001g0025 a0001c0002t0001g0352 a0001c0002t0004g0362 others(2): Show |
5 | NA18974.hp1 NA18981.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-10641T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617114 | |||||||
| chr2:241617119 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1241-10646A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617119 | |||||||
| chr2:241617280 | C | G | 3 | a0002c0004t0003g0159 a0002c0004t0003g0160 a0002c0004t0003g0161 |
3 | HG01081.hp1 HG01123.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1241-10807G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617280 | |||||||
| chr2:241617317 | G | A | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-10844C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617317 | |||||||
| chr2:241617435 | C | T | 1 | a0001c0002t0001g0354 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1241-10962G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617435 | |||||||
| chr2:241617592 | G | C | 1 | a0001c0002t0001g0336 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1241-11119C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617592 | |||||||
| chr2:241617604 | G | A | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-11131C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617604 | |||||||
| chr2:241617613 | G | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-11140C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617613 | |||||||
| chr2:241617717 | C | T | 1 | a0001c0002t0001g0290 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1241-11244G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617717 | |||||||
| chr2:241617764 | A | C | 136 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(133): Show |
140 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.1241-11291T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617764 | |||||||
| chr2:241617782 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-11309G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617782 | |||||||
| chr2:241617936 | A | T | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1241-11463T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241617936 | |||||||
| chr2:241618015 | T | G | 326 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(323): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1241-11542A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618015 | |||||||
| chr2:241618101 | C | T | 1 | a0002c0004t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1241-11628G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618101 | |||||||
| chr2:241618139 | C | T | 91 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(88): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1241-11666G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618139 | |||||||
| chr2:241618147 | T | C | 1 | a0002c0003t0001g0185 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1241-11674A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618147 | |||||||
| chr2:241618231 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1241-11758G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618231 | |||||||
| chr2:241618232 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
6 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-11759C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618232 | |||||||
| chr2:241618344 | T | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-11871A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618344 | |||||||
| chr2:241618370 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
188 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1241-11897A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618370 | |||||||
| chr2:241618512 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1241-12039C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618512 | |||||||
| chr2:241618540 | G | C | 1 | a0002c0004t0001g0076 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1241-12067C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618540 | |||||||
| chr2:241618603 | A | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1241-12130T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618603 | |||||||
| chr2:241618662 | C | T | 1 | a0001c0002t0001g0329 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1241-12189G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241618662 | |||||||
| chr2:241619168 | C | T | 1 | a0001c0002t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1241-12695G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619168 | |||||||
| chr2:241619172 | G | A | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1241-12699C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619172 | |||||||
| chr2:241619267 | G | C | 1 | a0001c0002t0001g0336 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1241-12794C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619267 | |||||||
| chr2:241619362 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1241-12889G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619362 | |||||||
| chr2:241619441 | G | A | 1 | a0002c0003t0001g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1241-12968C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619441 | |||||||
| chr2:241619499 | T | C | 9 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG02056.hp2 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-13026A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619499 | |||||||
| chr2:241619698 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+13219A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619698 | |||||||
| chr2:241619726 | C | CGGTGAGG others(4): Show |
1 | a0001c0002t0001g0012 | 2 | NA18943.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1240+13180_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619726 | |||||||
| chr2:241619756 | T | C | 359 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(356): Show |
385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.1240+13161A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619756 | |||||||
| chr2:241619782 | T | C | 2 | a0001c0001t0001g0140 a0002c0003t0001g0080 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+13135A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619782 | |||||||
| chr2:241619796 | G | T | 2 | a0001c0001t0001g0140 a0002c0003t0001g0080 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+13121C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619796 | |||||||
| chr2:241619831 | CGTGAGTG others(4): Show |
C | 94 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(91): Show |
94 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1240+13075_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619831 | |||||||
| chr2:241619842 | G | GGTGAGTG others(37): Show |
1 | a0001c0002t0001g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1240+13074_1240+13 others(50): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619842 | |||||||
| chr2:241619863 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0246 a0001c0001t0001g0247 others(14): Show |
19 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240+13054C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619863 | |||||||
| chr2:241619867 | CGGTGAGT others(4): Show |
C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0042 others(47): Show |
56 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1240+13039_1240+13 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619867 | |||||||
| chr2:241619938 | G | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(35): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1240+12979C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619938 | |||||||
| chr2:241619978 | CGGTGAGT others(4): Show |
C | 1 | a0001c0002t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1240+12928_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619978 | |||||||
| chr2:241619980 | GTGAGTGA others(27): Show |
G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+12903_1240+12 others(40): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619980 | |||||||
| chr2:241619990 | GGTGA | G | 96 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(93): Show |
96 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1240+12923_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241619990 | |||||||
| chr2:241620001 | C | T | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12916G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620001 | |||||||
| chr2:241620002 | A | G | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12915T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620002 | |||||||
| chr2:241620013 | G | A | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12904C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620013 | |||||||
| chr2:241620014 | A | G | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12903T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620014 | |||||||
| chr2:241620023 | GGGTGAGT others(1): Show |
G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12886_1240+12 others(14): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620023 | |||||||
| chr2:241620031 | T | G | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12886A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620031 | |||||||
| chr2:241620032 | G | GGTGAGTG others(4): Show |
9 | a0001c0001t0001g0217 a0002c0003t0001g0096 a0002c0003t0001g0188 others(6): Show |
9 | HG00544.hp2 HG00597.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+12874_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620032 | |||||||
| chr2:241620042 | G | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12875C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620042 | |||||||
| chr2:241620043 | A | AGTGAGTG others(4): Show |
3 | a0001c0002t0001g0205 a0002c0004t0001g0009 a0002c0004t0001g0071 |
4 | HG02818.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+12863_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | |||||||
| chr2:241620043 | A | C | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+12874T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | |||||||
| chr2:241620043 | A | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12874T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620043 | |||||||
| chr2:241620053 | G | C | 1 | a0001c0002t0001g0326 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1240+12864C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620053 | |||||||
| chr2:241620063 | G | GT | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12853_1240+12 others(7): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620063 | |||||||
| chr2:241620064 | G | C | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12853C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620064 | |||||||
| chr2:241620074 | GTCGT | G | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12839_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620074 | |||||||
| chr2:241620080 | A | G | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12837T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620080 | |||||||
| chr2:241620090 | G | A | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12827C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620090 | |||||||
| chr2:241620175 | GTGAGTCG others(20): Show |
G | 1 | a0001c0001t0001g0041 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1240+12715_1240+12 others(33): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620175 | |||||||
| chr2:241620182 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+12735C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620182 | |||||||
| chr2:241620193 | G | GGTGAGGA others(4): Show |
140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12713_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620193 | |||||||
| chr2:241620195 | TGAG | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12719_1240+12 others(9): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620195 | |||||||
| chr2:241620198 | GGAGT | G | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(31): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1240+12715_1240+12 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620198 | |||||||
| chr2:241620206 | TGAG | T | 3 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12708_1240+12 others(9): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620206 | |||||||
| chr2:241620210 | G | C | 3 | a0001c0001t0002g0048 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | NA18962.hp2 NA18984.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1240+12707C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620210 | |||||||
| chr2:241620234 | GGTGAGGA others(4): Show |
G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+12672_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620234 | |||||||
| chr2:241620270 | GGTGAGTG others(4): Show |
G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+12636_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620270 | |||||||
| chr2:241620281 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1240+12636G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620281 | |||||||
| chr2:241620304 | G | A | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12613C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620304 | |||||||
| chr2:241620326 | GGTGAGTG others(5): Show |
G | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+12579_1240+12 others(18): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620326 | |||||||
| chr2:241620365 | AGTGAGGG | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+12545_1240+12 others(13): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620365 | |||||||
| chr2:241620380 | G | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+12537C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620380 | |||||||
| chr2:241620425 | G | C | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+12492C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620425 | |||||||
| chr2:241620477 | T | TGGTGAGT others(15): Show |
1 | a0002c0003t0001g0080 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1240+12418_1240+12 others(28): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620477 | |||||||
| chr2:241620477 | TGGTGAGT others(4): Show |
T | 1 | a0001c0001t0001g0030 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1240+12429_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620477 | |||||||
| chr2:241620489 | A | AGTGAGTG others(4): Show |
4 | a0001c0002t0001g0354 a0001c0002t0001g0355 a0001c0002t0001g0356 others(1): Show |
4 | NA18939.hp2 NA18953.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+12417_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620489 | |||||||
| chr2:241620512 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG00438.hp1 HG00673.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1240+12405C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620512 | |||||||
| chr2:241620533 | C | T | 1 | a0002c0003t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1240+12384G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620533 | |||||||
| chr2:241620533 | CGGTGACT others(4): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1240+12373_1240+12 others(17): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620533 | |||||||
| chr2:241620614 | A | ATGAGTGA others(27): Show |
1 | a0002c0003t0001g0088 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1240+12269_1240+12 others(40): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620614 | |||||||
| chr2:241620728 | G | A | 1 | a0001c0002t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+12189C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620728 | |||||||
| chr2:241620729 | A | C | 1 | a0001c0002t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+12188T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620729 | |||||||
| chr2:241620742 | T | C | 1 | a0002c0003t0001g0097 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1240+12175A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620742 | |||||||
| chr2:241620826 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+12091G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620826 | |||||||
| chr2:241620877 | T | C | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+12040A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620877 | |||||||
| chr2:241620926 | T | C | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+11991A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241620926 | |||||||
| chr2:241621252 | G | A | 1 | a0001c0002t0001g0115 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1240+11665C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621252 | |||||||
| chr2:241621402 | T | C | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
143 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1240+11515A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621402 | |||||||
| chr2:241621471 | G | C | 1 | a0001c0002t0001g0337 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1240+11446C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621471 | |||||||
| chr2:241621530 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1240+11387A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621530 | |||||||
| chr2:241621585 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+11332G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621585 | |||||||
| chr2:241621608 | G | GA | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11308dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621608 | |||||||
| chr2:241621617 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11300C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621617 | |||||||
| chr2:241621632 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0065 others(1): Show |
5 | HG02145.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+11285C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621632 | |||||||
| chr2:241621664 | C | T | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+11253G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621664 | |||||||
| chr2:241621695 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.1240+11222T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621695 | |||||||
| chr2:241621708 | G | C | 1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1240+11209C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621708 | |||||||
| chr2:241621871 | G | A | 1 | a0001c0002t0001g0357 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1240+11046C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241621871 | |||||||
| chr2:241622054 | C | G | 2 | a0001c0001t0001g0131 a0002c0003t0001g0087 |
2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1240+10863G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622054 | |||||||
| chr2:241622059 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1240+10858T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622059 | |||||||
| chr2:241622096 | G | A | 144 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(141): Show |
149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1240+10821C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622096 | |||||||
| chr2:241622288 | A | C | 140 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(137): Show |
145 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1240+10629T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622288 | |||||||
| chr2:241622595 | C | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(217): Show |
232 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1240+10322G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622595 | |||||||
| chr2:241622596 | A | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0125 others(5): Show |
9 | HG01099.hp1 HG02145.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+10321T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622596 | |||||||
| chr2:241622746 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1240+10171A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622746 | |||||||
| chr2:241622883 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+10034C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622883 | |||||||
| chr2:241622960 | G | A | 2 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
2 | NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1240+9957C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241622960 | |||||||
| chr2:241623297 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+9620A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623297 | |||||||
| chr2:241623385 | G | C | 1 | a0002c0004t0001g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+9532C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623385 | |||||||
| chr2:241623451 | G | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(54): Show |
62 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1240+9466C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623451 | |||||||
| chr2:241623593 | G | GA | 39 | a0001c0001t0001g0065 a0001c0002t0001g0003 a0001c0002t0001g0004 others(36): Show |
43 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1240+9323dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623593 | |||||||
| chr2:241623607 | G | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0028 others(47): Show |
53 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1240+9310C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623607 | |||||||
| chr2:241623616 | C | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+9301G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241623616 | |||||||
| chr2:241624025 | G | A | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+8892C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624025 | |||||||
| chr2:241624101 | C | T | 5 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0002c0004t0001g0074 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+8816G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624101 | |||||||
| chr2:241624150 | A | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+8767T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624150 | |||||||
| chr2:241624356 | G | A | 3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1240+8561C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624356 | |||||||
| chr2:241624430 | T | C | 1 | a0001c0002t0001g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240+8487A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624430 | |||||||
| chr2:241624441 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1240+8476G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624441 | |||||||
| chr2:241624442 | G | A | 2 | a0001c0002t0001g0317 a0001c0002t0001g0318 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1240+8475C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624442 | |||||||
| chr2:241624485 | C | CA | 11 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(8): Show |
12 | HG02055.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1240+8431dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624485 | |||||||
| chr2:241624485 | CA | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0053 others(12): Show |
16 | HG01099.hp1 HG01884.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1240+8431delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624485 | |||||||
| chr2:241624598 | T | C | 4 | a0001c0002t0001g0306 a0001c0002t0001g0307 a0001c0002t0001g0308 others(1): Show |
4 | HG00408.hp1 NA18972.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+8319A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624598 | |||||||
| chr2:241624739 | G | A | 2 | a0002c0004t0003g0163 a0002c0004t0003g0164 |
2 | HG01261.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1240+8178C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624739 | |||||||
| chr2:241624887 | G | A | 1 | a0001c0002t0001g0344 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1240+8030C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624887 | |||||||
| chr2:241624956 | G | A | 31 | a0001c0002t0001g0276 a0001c0002t0001g0310 a0001c0002t0001g0311 others(28): Show |
31 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(28): Show |
intron_variant | MODIFIER | c.1240+7961C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241624956 | |||||||
| chr2:241625196 | C | T | 2 | a0002c0004t0001g0165 a0002c0004t0001g0170 |
2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1240+7721G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625196 | |||||||
| chr2:241625332 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1240+7585G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625332 | |||||||
| chr2:241625444 | T | C | 2 | a0001c0002t0001g0201 a0001c0002t0001g0202 |
2 | HG01934.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1240+7473A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625444 | |||||||
| chr2:241625481 | CA | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1240+7435delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625481 | |||||||
| chr2:241625481 | CAAAAAAA | C | 7 | a0001c0002t0001g0322 a0001c0002t0001g0323 a0001c0002t0001g0324 others(4): Show |
7 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+7429_1240+743 others(11): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625481 | |||||||
| chr2:241625495 | AAAAAGG | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+7416_1240+742 others(10): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625495 | |||||||
| chr2:241625711 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+7206A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625711 | |||||||
| chr2:241625797 | C | CA | 32 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(29): Show |
36 | HG00423.hp2 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1240+7119dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | |||||||
| chr2:241625797 | C | CAA | 10 | a0001c0001t0001g0057 a0001c0002t0001g0203 a0001c0002t0001g0210 others(7): Show |
10 | HG00642.hp1 HG00741.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+7118_1240+711 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | |||||||
| chr2:241625797 | CA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
133 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1240+7119delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | |||||||
| chr2:241625797 | CAA | C | 44 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(41): Show |
49 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1240+7118_1240+711 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625797 | |||||||
| chr2:241625807 | AAAAAAAA others(11): Show |
A | 1 | a0001c0002t0001g0200 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1240+7092_1240+710 others(22): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625807 | |||||||
| chr2:241625813 | A | AG | 89 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(86): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1240+7103_1240+710 others(5): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625813 | |||||||
| chr2:241625813 | A | G | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1240+7104T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625813 | |||||||
| chr2:241625818 | A | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+7099T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625818 | |||||||
| chr2:241625819 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1240+7098T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625819 | |||||||
| chr2:241625820 | A | G | 4 | a0001c0001t0001g0274 a0002c0003t0001g0019 a0002c0003t0001g0262 others(1): Show |
5 | HG02559.hp2 HG02622.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+7097T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625820 | |||||||
| chr2:241625845 | A | G | 1 | a0002c0003t0001g0177 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1240+7072T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241625845 | |||||||
| chr2:241626038 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1240+6879T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626038 | |||||||
| chr2:241626116 | G | C | 2 | a0001c0002t0001g0199 a0001c0002t0001g0200 |
2 | HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+6801C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626116 | |||||||
| chr2:241626223 | A | G | 1 | a0001c0002t0001g0281 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1240+6694T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626223 | |||||||
| chr2:241626224 | T | C | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+6693A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626224 | |||||||
| chr2:241626383 | G | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+6534C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626383 | |||||||
| chr2:241626490 | C | T | 1 | a0002c0004t0001g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1240+6427G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626490 | |||||||
| chr2:241626570 | G | GT | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0246 others(4): Show |
7 | HG01106.hp1 HG01255.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+6346dupA | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626570 | |||||||
| chr2:241626572 | T | G | 10 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(7): Show |
11 | HG02055.hp1 HG02818.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1240+6345A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626572 | |||||||
| chr2:241626614 | A | G | 1 | a0002c0004t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1240+6303T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626614 | |||||||
| chr2:241626753 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1240+6164T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626753 | |||||||
| chr2:241626762 | C | G | 93 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(90): Show |
93 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1240+6155G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626762 | |||||||
| chr2:241626762 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+6155G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626762 | |||||||
| chr2:241626888 | T | A | 1 | a0002c0003t0001g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1240+6029A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626888 | |||||||
| chr2:241626946 | CAT | C | 3 | a0001c0002t0001g0106 a0002c0004t0001g0074 a0002c0004t0001g0077 |
3 | HG01167.hp1 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1240+5969_1240+597 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241626946 | |||||||
| chr2:241627148 | T | C | 1 | a0001c0002t0001g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1240+5769A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627148 | |||||||
| chr2:241627178 | T | C | 95 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(92): Show |
95 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1240+5739A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627178 | |||||||
| chr2:241627291 | T | C | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+5626A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627291 | |||||||
| chr2:241627439 | C | A | 5 | a0002c0004t0003g0159 a0002c0004t0003g0160 a0002c0004t0003g0161 others(2): Show |
5 | HG01081.hp1 HG01123.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+5478G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627439 | |||||||
| chr2:241627490 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1240+5427G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627490 | |||||||
| chr2:241627792 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1240+5125G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627792 | |||||||
| chr2:241627934 | A | G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+4983T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627934 | |||||||
| chr2:241627955 | T | C | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1240+4962A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241627955 | |||||||
| chr2:241628060 | T | G | 1 | a0006c0007t0001g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+4857A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628060 | |||||||
| chr2:241628115 | A | G | 1 | a0002c0003t0001g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1240+4802T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628115 | |||||||
| chr2:241628234 | CCT | C | 44 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(41): Show |
48 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1240+4681_1240+468 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628234 | |||||||
| chr2:241628602 | G | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(54): Show |
62 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.1240+4315C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628602 | |||||||
| chr2:241628736 | C | CA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(47): Show |
55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1240+4180dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628736 | |||||||
| chr2:241628740 | AAAAAAAA others(8): Show |
A | 1 | a0001c0002t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+4162_1240+417 others(19): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628740 | |||||||
| chr2:241628747 | A | C | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+4170T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628747 | |||||||
| chr2:241628748 | CAAAAAAC others(10): Show |
C | 3 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0001g0153 |
3 | NA18963.hp2 NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1240+4152_1240+416 others(21): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628748 | |||||||
| chr2:241628769 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18979.hp2 NA19010.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1240+4148T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628769 | |||||||
| chr2:241628925 | C | CA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
117 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1240+3991dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | |||||||
| chr2:241628925 | C | CAA | 17 | a0001c0001t0001g0064 a0001c0001t0001g0070 a0001c0001t0001g0135 others(14): Show |
18 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240+3990_1240+399 others(6): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | |||||||
| chr2:241628925 | CA | C | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(138): Show |
147 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.1240+3991delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | |||||||
| chr2:241628925 | CAAAA | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3988_1240+399 others(8): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241628925 | |||||||
| chr2:241629125 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1240+3792G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629125 | |||||||
| chr2:241629234 | C | G | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240+3683G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629234 | |||||||
| chr2:241629287 | T | C | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+3630A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629287 | |||||||
| chr2:241629312 | A | T | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3605T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629312 | |||||||
| chr2:241629347 | T | C | 92 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1240+3570A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629347 | |||||||
| chr2:241629385 | G | C | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(354): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.1240+3532C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629385 | |||||||
| chr2:241629386 | G | A | 2 | a0001c0001t0001g0140 a0002c0003t0001g0080 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1240+3531C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629386 | |||||||
| chr2:241629463 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 |
5 | HG01934.hp2 NA18960.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+3454G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629463 | |||||||
| chr2:241629472 | TA | T | 109 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(106): Show |
109 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1240+3444delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629472 | |||||||
| chr2:241629929 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1240+2988T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629929 | |||||||
| chr2:241629936 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1240+2981C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629936 | |||||||
| chr2:241629960 | T | G | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+2957A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241629960 | |||||||
| chr2:241630146 | T | C | 1 | a0006c0007t0001g0072 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1240+2771A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630146 | |||||||
| chr2:241630153 | T | A | 1 | a0002c0003t0001g0195 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1240+2764A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630153 | |||||||
| chr2:241630198 | G | A | 2 | a0001c0002t0001g0004 a0001c0002t0001g0211 |
4 | HG01884.hp2 HG02109.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+2719C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630198 | |||||||
| chr2:241630215 | C | T | 2 | a0002c0005t0001g0154 a0002c0005t0001g0155 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1240+2702G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630215 | |||||||
| chr2:241630266 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1240+2651C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630266 | |||||||
| chr2:241630269 | G | A | 1 | a0001c0002t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1240+2648C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630269 | |||||||
| chr2:241630376 | C | CA | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+2540dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630376 | |||||||
| chr2:241630401 | C | A | 138 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+2516G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630401 | |||||||
| chr2:241630456 | A | C | 2 | a0001c0002t0001g0343 a0001c0002t0001g0344 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1240+2461T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630456 | |||||||
| chr2:241630473 | G | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1240+2444C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630473 | |||||||
| chr2:241630482 | T | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1240+2435A>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630482 | |||||||
| chr2:241630690 | A | AATTGCTT others(25): Show |
1 | a0001c0001t0001g0053 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1240+2195_1240+222 others(36): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630690 | |||||||
| chr2:241630779 | C | CA | 32 | a0001c0001t0001g0046 a0001c0001t0001g0128 a0001c0001t0001g0148 others(29): Show |
33 | HG00438.hp2 HG01928.hp2 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.1240+2137dupT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630779 | |||||||
| chr2:241630779 | CA | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0124 others(7): Show |
10 | HG01099.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1240+2137delT | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630779 | |||||||
| chr2:241630964 | T | C | 6 | a0001c0001t0001g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(3): Show |
6 | HG01981.hp1 HG02293.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+1953A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241630964 | |||||||
| chr2:241631026 | C | T | 139 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(136): Show |
144 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1240+1891G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631026 | |||||||
| chr2:241631030 | C | T | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+1887G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631030 | |||||||
| chr2:241631043 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG02132.hp2 NA18957.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1240+1874C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631043 | |||||||
| chr2:241631051 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
7 | HG01099.hp1 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+1866G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631051 | |||||||
| chr2:241631199 | G | A | 1 | a0001c0002t0001g0340 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1240+1718C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631199 | |||||||
| chr2:241631204 | G | A | 2 | a0001c0002t0001g0343 a0001c0002t0001g0344 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1240+1713C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631204 | |||||||
| chr2:241631297 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1240+1620A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631297 | |||||||
| chr2:241631424 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.1240+1493A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631424 | |||||||
| chr2:241631716 | C | T | 33 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0201 others(30): Show |
37 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1240+1201G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631716 | |||||||
| chr2:241631809 | G | T | 9 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG02056.hp2 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+1108C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631809 | |||||||
| chr2:241631816 | A | G | 4 | a0001c0002t0001g0199 a0001c0002t0001g0200 a0002c0005t0001g0154 others(1): Show |
4 | HG03209.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+1101T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631816 | |||||||
| chr2:241631868 | T | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+1049A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631868 | |||||||
| chr2:241631952 | AAG | A | 8 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+963_1240+964d others(4): Show |
THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631952 | |||||||
| chr2:241631967 | G | A | 137 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(134): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+950C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241631967 | |||||||
| chr2:241632130 | T | C | 1 | a0002c0003t0001g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1240+787A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632130 | |||||||
| chr2:241632133 | C | T | 9 | a0001c0002t0001g0024 a0001c0002t0001g0281 a0001c0002t0001g0282 others(6): Show |
9 | HG00639.hp1 HG01175.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+784G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632133 | |||||||
| chr2:241632279 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1240+638A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632279 | |||||||
| chr2:241632313 | T | C | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1240+604A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632313 | |||||||
| chr2:241632320 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1240+597C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632320 | |||||||
| chr2:241632422 | A | G | 137 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(134): Show |
142 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1240+495T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632422 | |||||||
| chr2:241632442 | A | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(36): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+475T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632442 | |||||||
| chr2:241632487 | C | G | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(36): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1240+430G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632487 | |||||||
| chr2:241632610 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1240+307T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632610 | |||||||
| chr2:241632638 | G | A | 1 | a0002c0003t0001g0197 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1240+279C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632638 | |||||||
| chr2:241632639 | G | C | 1 | a0002c0003t0001g0103 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240+278C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632639 | |||||||
| chr2:241632800 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1240+117A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632800 | |||||||
| chr2:241632847 | G | A | 21 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0203 others(18): Show |
25 | HG00423.hp2 HG00544.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1240+70C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632847 | |||||||
| chr2:241632881 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+36C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632881 | |||||||
| chr2:241632883 | A | G | 1 | a0001c0002t0001g0150 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1240+34T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 2/5 | chr2 | 241632883 | |||||||
| chr2:241634101 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-22C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634101 | |||||||
| chr2:241634102 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-23A>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634102 | |||||||
| chr2:241634103 | A | T | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.78-24T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634103 | |||||||
| chr2:241634182 | C | T | 1 | a0001c0002t0001g0276 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.78-103G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634182 | |||||||
| chr2:241634214 | C | A | 1 | a0001c0002t0001g0149 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.78-135G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634214 | |||||||
| chr2:241634228 | G | A | 1 | a0002c0004t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.78-149C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634228 | |||||||
| chr2:241634231 | C | T | 2 | a0002c0004t0001g0009 a0002c0004t0001g0071 |
3 | HG02818.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.78-152G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634231 | |||||||
| chr2:241634277 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.78-198C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634277 | |||||||
| chr2:241634353 | T | C | 3 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 |
3 | HG02559.hp1 HG02809.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.78-274A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634353 | |||||||
| chr2:241634494 | G | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-415C>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634494 | |||||||
| chr2:241634495 | C | T | 1 | a0002c0004t0005g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.78-416G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634495 | |||||||
| chr2:241634562 | G | C | 4 | a0001c0002t0001g0150 a0001c0002t0001g0151 a0001c0002t0001g0152 others(1): Show |
4 | NA18963.hp2 NA18967.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.78-483C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634562 | |||||||
| chr2:241634796 | T | C | 5 | a0001c0002t0001g0345 a0001c0002t0001g0346 a0001c0002t0001g0347 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-717A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634796 | |||||||
| chr2:241634894 | A | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
170 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.78-815T>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241634894 | |||||||
| chr2:241635088 | C | T | 86 | a0001c0002t0001g0276 a0001c0002t0001g0281 a0001c0002t0001g0282 others(83): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.78-1009G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635088 | |||||||
| chr2:241635257 | C | G | 3 | a0001c0002t0001g0351 a0001c0002t0001g0352 a0001c0002t0001g0353 |
3 | NA18948.hp2 NA19007.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.78-1178G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635257 | |||||||
| chr2:241635330 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01516.hp1 HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.78-1251T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635330 | |||||||
| chr2:241635391 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.78-1312C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635391 | |||||||
| chr2:241635416 | A | T | 1 | a0001c0001t0001g0021 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.78-1337T>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635416 | |||||||
| chr2:241635604 | C | T | 1 | a0002c0003t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.77+1337G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635604 | |||||||
| chr2:241635797 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.77+1144G>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635797 | |||||||
| chr2:241635807 | A | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
10 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.77+1134T>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635807 | |||||||
| chr2:241635850 | G | C | 1 | a0002c0003t0001g0244 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.77+1091C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635850 | |||||||
| chr2:241635876 | G | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
7 | HG01934.hp2 NA18960.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.77+1065C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635876 | |||||||
| chr2:241635886 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02074.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.77+1055A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241635886 | |||||||
| chr2:241636141 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0246 a0001c0001t0001g0247 others(30): Show |
36 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.77+800A>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636141 | |||||||
| chr2:241636386 | G | A | 7 | a0001c0002t0001g0351 a0001c0002t0001g0352 a0001c0002t0001g0353 others(4): Show |
7 | NA18939.hp2 NA18948.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+555C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636386 | |||||||
| chr2:241636401 | G | A | 87 | a0001c0002t0001g0276 a0001c0002t0001g0281 a0001c0002t0001g0282 others(84): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.77+540C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636401 | |||||||
| chr2:241636545 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.77+396C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636545 | |||||||
| chr2:241636648 | G | A | 1 | a0002c0004t0001g0359 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.77+293C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636648 | |||||||
| chr2:241636697 | C | G | 41 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.77+244G>C | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636697 | |||||||
| chr2:241636701 | C | T | 1 | a0002c0004t0001g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.77+240G>A | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636701 | |||||||
| chr2:241636719 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.77+222C>T | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636719 | |||||||
| chr2:241636853 | G | C | 1 | a0001c0002t0001g0361 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.77+88C>G | THAP4 | ENSG00000176946.13 | transcript | ENST00000407315.6 | protein_coding | 1/5 | chr2 | 241636853 |